ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-0025 CPXCR1 SNP Missense_Mutation 23 88008469 T G 52 63 HNSC HN_00466 CPXCR1 SNP Missense 23 88008900 C T 32 49 LUAD LUAD-B02594 CPXCR1 SNP Missense_Mutation 23 88008602 G T 48 57 LUAD LUAD-F00121 CPXCR1 SNP Missense_Mutation 23 88009103 C A 23 57 LUAD LUAD-F00162 CPXCR1 SNP Missense_Mutation 23 88008758 G T 35 55 LUAD LUAD-F00368 CPXCR1 SNP Missense_Mutation 23 88008831 G C 33 55 LUAD LUAD-RT-S01813 CPXCR1 SNP Missense_Mutation 23 88008911 G T 35 45 MEL ME010 CPXCR1 SNP Missense_Mutation 23 88009065 T A 64 49 MEL MEL-JWCI-WGS-1 CPXCR1 SNP Missense_Mutation 23 88008663 A C 9 64 MEL MEL-JWCI-WGS-1 CPXCR1 SNP Missense_Mutation 23 88008728 C T 26 33 MEL MEL-Ma-Mel-119 CPXCR1 SNP Missense_Mutation 23 88009089 G A 43 45 MEL MEL-Ma-Mel-36 CPXCR1 SNP Missense_Mutation 23 88008632 G A 37 57 MEL MEL-Ma-Mel-36 CPXCR1 SNP Missense_Mutation 23 88009059 G A 41 52 MEL MEL-Ma-Mel-65 CPXCR1 SNP Missense_Mutation 23 88008767 G A 45 51 MM MM-0487 CPXCR1 SNP Silent 23 88008631 C T 31 51 LUAD TCGA-05-4410 CPXCR1 SNP Nonsense_Mutation 23 88008656 C T 19 56 LUAD TCGA-05-4427 CPXCR1 SNP Missense_Mutation 23 88008723 A G 6 48 GBM TCGA-06-0173 CPXCR1 SNP Missense_Mutation 23 88009244 T C 56 47 OV TCGA-13-1495 CPXCR1 SNP Nonsense_Mutation 23 88008812 C T 31 65 LUAD TCGA-17-Z014 CPXCR1 SNP Silent 23 88008697 C A 22 39 LUSC TCGA-18-5592 CPXCR1 SNP Missense_Mutation 23 88008875 C A 21 55 OV TCGA-23-1024 CPXCR1 SNP Missense_Mutation 23 88008468 A T 4 54 OV TCGA-36-1568 CPXCR1 SNP Missense_Mutation 23 88009031 C T 23 51 LUSC TCGA-37-3783 CPXCR1 SNP Missense_Mutation 23 88008729 C A 22 51 LUAD TCGA-44-4112 CPXCR1 SNP Missense_Mutation 23 88008704 C G 30 56 LUAD TCGA-44-6774 CPXCR1 SNP Missense_Mutation 23 88008572 C A 26 48 LUAD TCGA-44-6778 CPXCR1 SNP Missense_Mutation 23 88009303 C G 25 53 LUAD TCGA-49-6767 CPXCR1 SNP Nonsense_Mutation 23 88009014 C A 31 48 LUSC TCGA-60-2698 CPXCR1 SNP Missense_Mutation 23 88009209 T C 60 49 LUSC TCGA-60-2710 CPXCR1 SNP Nonsense_Mutation 23 88008902 C T 29 51 LUSC TCGA-60-2722 CPXCR1 SNP Missense_Mutation 23 88009119 C A 32 57 LUAD TCGA-64-1678 CPXCR1 DNP Missense_Mutation 23 88009116 GG TT 35 67 LUAD TCGA-67-3771 CPXCR1 SNP Missense_Mutation 23 88008905 G T 42 32 LUSC TCGA-70-6722 CPXCR1 SNP Missense_Mutation 23 88009035 C A 22 55 LUAD TCGA-73-4662 CPXCR1 SNP Missense_Mutation 23 88008550 A T 1 48 LUAD TCGA-75-6211 CPXCR1 SNP Missense_Mutation 23 88008544 G T 35 52 BRCA TCGA-A2-A04Y CPXCR1 SNP Missense_Mutation 23 88008777 C T 25 40 CRC TCGA-A6-2672 CPXCR1 SNP Missense_Mutation 23 88008450 C T 28 47 CRC TCGA-AA-3555 CPXCR1 SNP Missense_Mutation 23 88009005 G T 33 64 CRC TCGA-AA-A010 CPXCR1 SNP Missense_Mutation 23 88008449 G A 34 47 CRC TCGA-AA-A010 CPXCR1 SNP Missense_Mutation 23 88008711 A C 1 63 CRC TCGA-AA-A01T CPXCR1 SNP Missense_Mutation 23 88008648 A T 1 64 CRC TCGA-AA-A01X CPXCR1 SNP Missense_Mutation 23 88009032 G A 40 38 CRC TCGA-AF-3913 CPXCR1 SNP Silent 23 88008496 T C 57 55 CRC TCGA-AG-3892 CPXCR1 SNP Missense_Mutation 23 88009305 G T 34 45 CRC TCGA-AG-A008 CPXCR1 SNP Missense_Mutation 23 88009103 C T 23 57 CRC TCGA-AG-A02N CPXCR1 INS Frame_Shift_Ins 23 88008695 - C 10 54 UCEC TCGA-AP-A056 CPXCR1 SNP Missense_Mutation 23 88008976 C A 29 49 UCEC TCGA-AP-A0LM CPXCR1 SNP Missense_Mutation 23 88008449 G A 34 47 UCEC TCGA-AP-A0LM CPXCR1 SNP Missense_Mutation 23 88009014 C T 31 48 UCEC TCGA-AP-A0LM CPXCR1 SNP Missense_Mutation 23 88009116 G T 35 67 BRCA TCGA-AR-A250 CPXCR1 SNP Missense_Mutation 23 88008722 C T 29 50 UCEC TCGA-AX-A060 CPXCR1 SNP Silent 23 88008595 A G 3 52 KIRC TCGA-B0-5107 CPXCR1 SNP Missense_Mutation 23 88009260 G A 41 67 UCEC TCGA-B5-A0JY CPXCR1 SNP Nonsense_Mutation 23 88008938 C T 27 55 HNSC TCGA-BB-4223 CPXCR1 SNP Missense_Mutation 23 88008677 G C 33 47 HNSC TCGA-BB-7863 CPXCR1 SNP Missense_Mutation 23 88008652 T A 50 46 UCEC TCGA-BS-A0UV CPXCR1 SNP Missense_Mutation 23 88008598 T G 51 54 UCEC TCGA-BS-A0UV CPXCR1 SNP Silent 23 88008631 C T 31 51 UCEC TCGA-BS-A0UV CPXCR1 SNP Missense_Mutation 23 88009229 A C 13 51 HNSC TCGA-CN-4739 CPXCR1 SNP Missense_Mutation 23 88009098 G T 33 49 HNSC TCGA-CN-5364 CPXCR1 SNP Missense_Mutation 23 88008565 C A 17 39 HNSC TCGA-CR-6484 CPXCR1 SNP Missense_Mutation 23 88008988 G C 33 42 HNSC TCGA-CV-5439 CPXCR1 SNP Missense_Mutation 23 88008503 G C 33 56 HNSC TCGA-CV-7245 CPXCR1 SNP Nonsense_Mutation 23 88009299 C A 29 57 UCEC TCGA-D1-A16X CPXCR1 SNP Missense_Mutation 23 88009062 A C 1 49 UCEC TCGA-D1-A17Q CPXCR1 SNP Silent 23 88008631 C T 31 51 UCEC TCGA-D1-A17Q CPXCR1 SNP Silent 23 88008718 C A 32 47 BLCA TCGA-G2-A2EJ CPXCR1 SNP Missense_Mutation 23 88008581 G T 34 29